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  • Enantiomerically pure P-chiral phosphinoselenoic chlorides: inversion of configuration at the P-chirogenic center in the synthesis and reaction of these substances.

Enantiomerically pure P-chiral phosphinoselenoic chlorides: inversion of configuration at the P-chirogenic center in the synthesis and reaction of these substances.

Chemical communications (Cambridge, England) (2005-08-11)
Tsutomu Kimura, Toshiaki Murai
ABSTRACT

Reaction of diastereomerically pure phosphinoselenoic acid salts with oxalyl chloride leads to enantiomerically pure P-chiral phosphinoselenoic chlorides with inversion of configuration at phosphorus; one of these chlorides is converted to a phosphinoselenothioic acid salt with a high degree of enantioselectivity.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Oxalyl chloride, reagent grade, 98%
Sigma-Aldrich
Oxalyl chloride, ReagentPlus®, ≥99%
Sigma-Aldrich
Oxalyl chloride solution, 2.0 M in methylene chloride